Boronic acid, B-4-piperidinyl-
PIPERIDINE-4-BORONIC ACID
CAS: 120347-72-0
Molecular Formula: C5H12BNO2
Boronic acid, B-4-piperidinyl- - Names and Identifiers
| Name | PIPERIDINE-4-BORONIC ACID |
| Synonyms | PIPERIDINE-4-BORONIC ACID Piperidin-4-ylboronic acid Boronic acid, 4-piperidinyl- Boronic acid, B-4-piperidinyl- |
| CAS | 120347-72-0 |
Boronic acid, B-4-piperidinyl- - Physico-chemical Properties
| Molecular Formula | C5H12BNO2 |
| Molar Mass | 128.97 |
| Density | 1.08±0.1 g/cm3(Predicted) |
| Boling Point | 280.8±50.0 °C(Predicted) |
| pKa | 9.96±0.20(Predicted) |
| Storage Condition | 2-8℃ |
Boronic acid, B-4-piperidinyl- - Upstream Downstream Industry
| Raw Materials | Pyridine-4-boronic acid |
| Downstream Products | PIPERIDINE-3-BORONIC ACID tert-butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)piperidine-1-carboxylate |
Boronic acid, B-4-piperidinyl- - Introduction
PIPERIDINE-4-BORONIC ACID is an organic compound with the chemical formula C5H10BNO2.
Nature:
PIPERIDINE-4-BORONIC ACID is a colorless solid, soluble in water and organic solvents. It has high thermal and chemical stability.
Use:
PIPERIDINE-4-BORONIC ACID is an important intermediate in organic synthesis. It is widely used in the fields of medicine, pesticide and material science. In organic synthesis, it is often used to synthesize other compounds, such as ligands of organometallic catalysts, precursors of drug molecules, etc.
Method:
There are many preparation methods of PIPERIDINE-4-BORONIC ACID, but the most common preparation method is obtained by the reaction of piperidin-4-ol and triphenylboron. In the specific operation, piperidin-4-ol reacts with triphenylboron in an inert atmosphere to generate PIPERIDINE-4-BORONIC ACID.
Safety Information:
PIPERIDINE-4-BORONIC ACID has no obvious harm to human body and environment under normal use conditions. However, as a chemical substance, it should follow the general safety test practice, such as wearing appropriate personal protective equipment (gloves, protective glasses, etc.), prevent contact with skin and inhalation of dust or gas. Keep away from ignition and oxidizing agents during use or storage. In the case of accidental leakage or ingestion, seek medical help immediately.
Nature:
PIPERIDINE-4-BORONIC ACID is a colorless solid, soluble in water and organic solvents. It has high thermal and chemical stability.
Use:
PIPERIDINE-4-BORONIC ACID is an important intermediate in organic synthesis. It is widely used in the fields of medicine, pesticide and material science. In organic synthesis, it is often used to synthesize other compounds, such as ligands of organometallic catalysts, precursors of drug molecules, etc.
Method:
There are many preparation methods of PIPERIDINE-4-BORONIC ACID, but the most common preparation method is obtained by the reaction of piperidin-4-ol and triphenylboron. In the specific operation, piperidin-4-ol reacts with triphenylboron in an inert atmosphere to generate PIPERIDINE-4-BORONIC ACID.
Safety Information:
PIPERIDINE-4-BORONIC ACID has no obvious harm to human body and environment under normal use conditions. However, as a chemical substance, it should follow the general safety test practice, such as wearing appropriate personal protective equipment (gloves, protective glasses, etc.), prevent contact with skin and inhalation of dust or gas. Keep away from ignition and oxidizing agents during use or storage. In the case of accidental leakage or ingestion, seek medical help immediately.
Last Update：2024-04-09 15:18:02
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Product Name: PIPERIDINE-4-BORONIC ACID Visit Supplier Webpage Request for quotation
CAS: 120347-72-0
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
Wechat: 18301782025
CAS: 120347-72-0
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
Wechat: 18301782025
View History
Raw Materials for Boronic acid, B-4-piperidinyl-
Downstream Products for Boronic acid, B-4-piperidinyl-
PIPERIDINE-3-BORONIC ACID
tert-butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)piperidine-1-carboxylate
tert-butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)piperidine-1-carboxylate